Reported Feb 18, 2026 · Ongoing
Reprocessed Abbott Inquiry Steerable Diagnostic Catheters
Medline Industries, LP
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medline Industries, LP · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
Reprocessed Abbott Inquiry Steerable Diagnostic Catheters
7 of 7 products
| # | Product as published |
|---|---|
| 1 | Abbott Inquiry Steerable Diagnostic Catheter 10 Elec. 2-5-2mm 81105RH 81172RH |
| 2 | Abbott Inquiry Steerable Diagnostic Catheter 20 Elec. 2-10-2mm 81202RH |
| 3 | Abbott Inquiry Steerable Diagnostic Catheter 4 Elec. 5mm 81483RH |
| 4 | Inquiry Steerable Diagnostic Catheter 10 Elec. 2-5-2mm 81102RH 81104RH 81174RH 81531RH 81532RH |
| 5 | Inquiry Steerable Diagnostic Catheter 10 Elec. 5mm 81107RH |
| 6 | Inquiry Steerable Diagnostic Catheter 4 Elec. 2-5-2mm 81402RH 81404RH 81405RH 81474RH |
| 7 | Inquiry Steerable Diagnostic Catheter 4 Elec. 5mm 81473RH |
- Lot codes and dates
15 of 15 products
Products covered by this recall # Barcodes Product as published 1 10197344133284Lot EP250618; 81172RH UDI-DI 10197344133284 2 10197344133307Lot EP250618; 81202RH UDI-DI 10197344133307 3 10197344133444Lot EP250618; 81483RH UDI-DI 10197344133444 4 2019734413323610197344133239Lot EP250618; 81102RH UDI-DI (case) 20197344133236¿ (ea) 10197344133239 5 10197344133246Lot EP250618; 81104RH UDI-DI 10197344133246 6 10197344133291Lot EP250618; 81174RH UDI-DI 10197344133291 7 10197344133512Lot EP250618; 81531RH UDI-DI 10197344133512 8 10197344133529Lot EP250618; 81532RH UDI-DI 10197344133529 9 10197344133260Lot EP250618; 81107RH UDI-DI 10197344133260 10 10197344133352Lot EP250618; 81402RH UDI-DI 10197344133352 11 10197344133376Lot EP250618; 81404RH UDI-DI 10197344133376 12 10197344133383Lot EP250618; 81405RH UDI-DI 10197344133383 13 10197344133437Lot EP250618; 81474RH UDI-DI 10197344133437 14 10197344133420Lot EP250618; 81473RH UDI-DI 10197344133420 15 Lot EP250618 - Amount recalled
- 311
This recall covers 20 products
The agency filed one notice per product. You are reading one of them; the other 19 are below.
7 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025
Using this product could cause serious injury, illness or death — stop using it now.
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